DISEASES - autosomal dominant nonsyndromic deafness 59

Human genes for autosomal dominant nonsyndromic deafness 59

Autosomal dominant nonsyndromic deafness 59 [DOID:0110583]

An autosomal dominant nonsyndromic deafness that has_material_basis_in variation in the chromosome region 11p14.2-q12.3.

Synonyms: autosomal dominant nonsyndromic deafness 59, DOID:0110583, autosomal dominant deafness 59, DFNA59

The disease-gene associations are derived from automatic text mining of the biomedical literature, manually curated database annotations, cancer mutation data, and genome-wide association studies. The confidence of each association is signified by stars, where ★★★★★ is the highest confidence and ★☆☆☆☆ is the lowest.

Developed by Sune Frankild, Alexander Junge, Albert Pallejà, Dhouha Grissa, Kalliopi Tsafou, and Lars Juhl Jensen from the Novo Nordisk Foundation Center for Protein Research.